Ira Seth Winer
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Ira Seth Winer has a total of 194 co-authors. Here are the top co-authors by number of shared publications:
- Joanne Xiu
Caris Life Sciences, Phoenix, Arizona, USA
45 shared publications - Nathaniel Jones
Mitchell Cancer Institute University of South Alabama, Mobile, AL, United States
41 shared publications - Anthony F. Shields
Karmanos Cancer Institute, Wayne State University, Detroit, Michigan
40 shared publications - David Spetzler
Caris Life Sciences, Phoenix, USA
40 shared publications - Elisabeth I. Heath
Mayo Clinic Rochester Minnesota USA
40 shared publications - Frank Cameron Cackowski
Barbara Ann Karmanos Cancer Institute, Wayne State University, Detroit, USA
40 shared publications
Latest Publications
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S8 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Comparison of overall survival among chemotherapy-treated TP53-mutated and TP53-wild type patients in Caris CODEai clinico-genomic database
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S8 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Comparison of overall survival among chemotherapy-treated TP53-mutated and TP53-wild type patients in Caris CODEai clinico-genomic database
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S3 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
COXPH model for patients with stage information
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S3 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
COXPH model for patients with stage information
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S5 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Copy number alterations (CNAs) and fusions among cohort
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S5 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Copy number alterations (CNAs) and fusions among cohort
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Fiugre S4 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Overall survival by RUCA code and poverty
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Fiugre S4 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Overall survival by RUCA code and poverty
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S2 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
COXPH model for patients with at least 6-mo overall survival
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S2 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
COXPH model for patients with at least 6-mo overall survival
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S1 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Comparison of Caris cohort data with Puckrein dataset
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S1 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Comparison of Caris cohort data with Puckrein dataset
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S7 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Gene mutations according to poverty level and RUCA codes
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S7 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Gene mutations according to poverty level and RUCA codes
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S2 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Overall survival of cohort by stage
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S2 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Overall survival of cohort by stage
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S6 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Prevalence of common mutations in tumor subtypes
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S6 from Health Disparities among Patients with Cancer Who Received Molecular Testing for Biomarker-Directed Therapy
Prevalence of common mutations in tumor subtypes